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Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Simurda T, Brunclikova M, Asselta R, Caccia S, Zolkova J, Kolkova Z, Loderer D, Skornova I, Hudecek J, Lasabova Z, Stasko J, Kubisz P. Simurda T, et al. Among authors: kubisz p. Int J Mol Sci. 2020 Jun 29;21(13):4616. doi: 10.3390/ijms21134616. Int J Mol Sci. 2020. PMID: 32610551 Free PMC article. Review.
A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype.
Simurda T, Vilar R, Zolkova J, Ceznerova E, Kolkova Z, Loderer D, Neerman-Arbez M, Casini A, Brunclikova M, Skornova I, Dobrotova M, Grendar M, Stasko J, Kubisz P. Simurda T, et al. Among authors: kubisz p. Biomedicines. 2020 Dec 13;8(12):605. doi: 10.3390/biomedicines8120605. Biomedicines. 2020. PMID: 33322159 Free PMC article.
Yes or no for secondary prophylaxis in afibrinogenemia?
Simurda T, Stanciakova L, Stasko J, Dobrotova M, Kubisz P. Simurda T, et al. Among authors: kubisz p. Blood Coagul Fibrinolysis. 2015 Dec;26(8):978-80. doi: 10.1097/MBC.0000000000000392. Blood Coagul Fibrinolysis. 2015. PMID: 26484644 No abstract available.
223 results